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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782578Generated: October 30, 2026

Diisopropylethylamine → HCID 68972293, compound

https://huagongshe.com/reaction/1782578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 88438—
ReactantHCID 68975066HCID 68975066—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68972293HCID 6897229339%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of the above nitrile (0.20 g, 0.65 mmol) and nicotinoyl chloride hydrochloride (0.46 g, 2.6 mmol) in THF (6 mL) was then treated with DIPEA (0.56 mL, 3.2 mmol) and stirred at 80° C. for 16 h. The reaction was cooled to room temperature, concentrated under reduced pressure, diluted with CH2Cl2 (10 mL) and washed with brine solution (2×10 mL). The combined organic extracts were then dried (Na2SO4), filtered and concentrated and the crude material purified by flash column chromatography on silica gel (50:1:0.1 CH2Cl2/MeOH/NH4OH) to afford N-[(R)-1-(2-cyano-1-methyl-ethyl)-piperidin-4-yl]-N-(4-difluoromethoxy-phenyl)-nicotinamide as a pale yellow oil (104 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498346B2
Source datasetuspto-grants-2009_03
ORD IDord-509ba96307904656baf9865e99f729ea
Source noteuspto-grants-2009_03